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BriaCell Reports Positive Survival Data in Advanced Metastatic Breast Cancer 9 of 11 women remain alive from 2021/2022 dosing, highlighting strong survival benefits. Remains well tolerated with no dose limiting toxicitie

Key Takeaway: BriaCell Therapeutics Corp. has reported promising survival data from their Phase II clinical trial for advanced metastatic breast cancer. Following treatment, 9 out of 11 patients from the previously dosed group remain alive, which the company cites as strong evidence of survival benefits. The regimen, which combines Bria-IMT with Incyte's retifanlimab, is well tolerated, with no adverse dose limiting toxicities observed. Furthermore, 64% of participants demonstrated either disease control or progression-free survival, indicating potential clinical effectiveness within this challenging patient population.

Market Sentiment Analysis

POSITIVE FACTORS

  • 9 out of 11 patients remain alive from 2021/2022 dosing, indicating strong survival benefits.
  • The treatment is well tolerated with no dose limiting toxicities reported.
  • 64% of patients experienced disease control or progression-free survival benefits.
  • Potentially better responding subgroups of patients are identified, representing a large segment of advanced breast cancer patients.

Full Press Release Details

Reports Positive Survival Data in Advanced Metastatic Breast Cancer
9 of 11 women remain alive from 2021/2022 dosing, highlighting strong survival benefits.
Remains well tolerated with no dose limiting toxicities.
Primary endpoint in pending pivotal trial will be survival, as agreed by the FDA.
9 additional patients have been screened/enrolled in the study, incremental to the 12 patients announced in December 2022.
PA and VANCOUVER, British Columbia, February 23, 2023- BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW) (TSX: BCT) ("BriaCell"
or the "Company"), a clinical-stage biotechnology company specializing in targeted immunotherapies for cancer, today reports
updated survival data from its previously disclosed group of 12 patients (11 patients enrolled in 2021/2022) in the ongoing Phase
II clinical trial evaluating Bria-IMT in combination with Incyte's retifanlimab for the treatment of advanced metastatic
9 of 11 (82%) patients remain alive from 2021/2022 dosing, suggesting strong survival benefits.
7 of 11 (64%) patients showed either disease control or progression-free survival ("PFS") benefits compared with their most recent prior therapy regimen suggesting clinical benefit, including survival and delayed cancer progression in this very difficult to treat patient population.
Median PFS of 3.5 months (with one subject ongoing) compares favorably with other recent studies of patients with advanced disease including other approved agents in earlier lines of therapy (Tripathy "ATTAIN" 2022, Perez 2015 "BEACON", Cortes 2018, O'Shaughnessy 2022 "ASCENT").
Regimen remains well tolerated with no dose limiting toxicities.
is working, and it's working well. We had high hopes going into this clinical read-out, and the survival numbers have even
exceeded our expectations. With 9 of 11 women still alive, this has a material impact for the patients and their loved ones, especially
since some patients may have had only weeks or months to live prior to our treatment," stated Dr. William V. Williams, BriaCell's
President and CEO. "This survival update bodes well for our upcoming pivotal trial, since the FDA has agreed to survival benefits
as the primary endpoint."
clinical data from BriaCell's combination regimen highlights survival benefits in a cohort (3rd line or later) with
a life expectancy of merely months or weeks in some cases. Patients in this cohort had failed a
median of 5 other treatments prior to enrolling in BriaCell's study. Other reportable benefits such as less pain and better
quality of life were also observed in these patients.
of top-responding patients: 4 of 5 patients with Grade I/II cancer, and 6 of 8 hormone receptor positive (HR+) patients had either
disease control or improved PFS suggesting potentially better responding subgroup/s of patients. These subgroups
represent large segments of the advanced breast cancer patient population.
update: 9 additional patients have been screened/enrolled in the study, incremental to the
12 patients announced in December 2022. With patients continuing to enroll and remain on the treatment, more data including overall survival
data will be disclosed at regular intervals.
BriaCell Therapeutics Corp.
is an immuno-oncology-focused biotechnology company developing targeted and effective approaches for the management of cancer. More information
is available at https://briacell.com/.
press release contains "forward-looking statements" that are subject to substantial risks and uncertainties. All statements,
other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements
contained in this press release may be identified by the use of words such as "anticipate," "believe," "contemplate,"
"could," "estimate," "expect," "intend," "seek," "may," "might,"
"plan," "potential," "predict," "project," "target," "aim," "should,"
"will," "would," or the negative of these words or other similar expressions, although not all forward-looking
statements contain these words. Forward-looking statements are based on BriaCell's current expectations and are subject to inherent
uncertainties, risks, and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions
as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully under the heading
"Risks and Uncertainties" in the Company's most recent Management's Discussion and Analysis, under the heading
"Risk Factors" in the Company's most recent Annual Information Form, and under "Risks and Uncertainties"
in the Company's other filings with the Canadian securities regulatory authorities and the U.S. Securities and Exchange Commission,
all of which are available under the Company's profiles on SEDAR at www.sedar.com and on EDGAR at www.sec.gov.
Forward-looking statements contained in this announcement are made as of this date, and BriaCell Therapeutics Corp. undertakes no duty
to update such information except as required under applicable law.
the Toronto Stock Exchange nor its Regulation Services Provider (as that term is defined in the policies of the Toronto Stock Exchange)
accepts responsibility for the adequacy or accuracy of this release.

Frequently Asked Questions

What is the survival rate from the 2021/2022 dosing?

82% of patients, or 9 out of 11, remain alive from the 2021/2022 dosing.

How well is Bria-IMT tolerated by patients?

The regimen is well tolerated with no dose limiting toxicities reported.

What is the primary endpoint of the pivotal trial?

The FDA has agreed that survival benefits will be the primary endpoint.

How many additional patients were enrolled in the study?

9 additional patients have been screened and enrolled in the study.

What are the observed benefits for patients?

Benefits include disease control, improved PFS, less pain, and better quality of life.

Last updated: Feb 23, 2023